Epitope-Tagged Pkhd1 Tracks the Processing, Secretion, and Localization of Fibrocystin

Mutations in the PKHD1 gene, which encodes fibrocystin, cause autosomal recessive polycystic kidney disease (ARPKD). Unfortunately, the lack of specific antibodies to the mouse protein impairs the study of splicing, post-translational processing, shedding, and temporal and spatial expression of endo...

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Detalhes bibliográficos
Main Authors: Bakeberg, Jason L., Tammachote, Rachaneekorn, Woollard, John R., Hogan, Marie C., Tuan, Han-Fang, Li, Ming, van Deursen, Jan M., Wu, Yanhong, Huang, Bing Q., Torres, Vicente E., Harris, Peter C., Ward, Christopher J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2011
Assuntos:
Basic Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3250208/
https://ncbi.nlm.nih.gov/pubmed/22021705
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2010111173
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